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Titlebook: Gene Therapy for Cancer; Kelly K. Hunt,Stephan A. Vorburger,Stephen G. Swis Book 2007 Humana Press 2007 angiogenesis.apoptosis.cancer trea

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书目名称Gene Therapy for Cancer
编辑Kelly K. Hunt,Stephan A. Vorburger,Stephen G. Swis
视频video
概述Vectors used in gene therapy for cancer.Characteristics and production methods of cancer gene vectors.Targets and specific approaches for the therapy of cancer.Clinical applications of cancer gene the
丛书名称Cancer Drug Discovery and Development
图书封面Titlebook: Gene Therapy for Cancer;  Kelly K. Hunt,Stephan A. Vorburger,Stephen G. Swis Book 2007 Humana Press 2007 angiogenesis.apoptosis.cancer trea
描述The possibility of treating cancer, a disease defined by genetic defects, by introducing genes targeting these very alterations has led to an immense interest in gene therapy for cancer. Although incremental successes have been realized, enthusiasm for gene therapy has declined due to an increasing number of obstacles. These obstacles include vector systems that do not reach systemic metastases, therapeutic genes with redundant mec- nisms allowing for cellular resistance, and toxicities in clinical trials leading to premature closure of these studies. Different tactics to overcome or circumvent these obstacles have catalyzed the development of a wide range of gene therapy approaches. Thus far, almost two-thirds of gene therapy trials have focused on cancer. This reflects the concept that gene therapy approaches for the treatment of cancer do not necessarily require long-term expression of the gene as is necessary for the treatment of primary genetic defects like hemophilia or juvenile diabetes. Unlike the treatment of genetic defects, where expr- sion of the corrected gene needs to be strong, permanent and, sometimes regulated, tactics to treat tumors can be based on temporary and
出版日期Book 2007
关键词angiogenesis; apoptosis; cancer treatment; clinical trial; gene therapy; gene transfer; hematopoietic stem
版次1
doihttps://doi.org/10.1007/978-1-59745-222-9
isbn_softcover978-1-61737-590-3
isbn_ebook978-1-59745-222-9Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightHumana Press 2007
The information of publication is updating

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Rigid bodies and non-inertial frames,from low-level Ad receptor expression and/or anatomical barriers, including extracellular matrix surrounding tumors, have established a great need for research to further improve existing Ad vectors and unravel their true therapeutic potential as anticancer agents. This chapter reviews and discusses
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Classical Systems in Quantum Mechanicsc gene products have been evaluated as tools for amplifying or enriching gene-modified HSCs in vivo. These include the homeobox transcription factors, selective amplifier genes, and drug resistance genes. The ability to enrich and repopulate the hematopoietic compartment with therapeutic gene-correc
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Combination of Gene Therapy with Radiationrated significant potential for the combination of cancer gene therapy with radiotherapy that could lead to improved treatment responses. This chapter attempts to highlight some of the gene therapy approaches that have shown success both in preclinical models and in clinical trials when used in comb
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